Prognostic Factors for Survival in Adults With Burkitt Lymphoma: A Systematic Review

IF 3.1 2区 医学 Q2 ONCOLOGY Cancer Medicine Pub Date : 2025-01-29 DOI:10.1002/cam4.70513
Aythami de Armas-Castellano, Diego Infante-Ventura, Tasmania del Pino-Sedeño, Yadira González Hernández, Raul Quiros, Beatriz León-Salas, Vincent Ribrag, María M. Trujillo-Martín, ERN EuroBlood Working Group
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Abstract

Introduction

Burkitt lymphoma (BL) is a rare and aggressive subtype of non-Hodgkin's lymphoma. Several studies have identified prognostic factors (PFs) for disease progression and mortality among adults with BL. However, there is no consensus on risk stratification based on PFs. This study aims to identify, critically assess, and synthesize the available evidence on PFs for survival in adults with BL.

Methods

A systematic review was conducted. Medline, EMBASE, and CENTRAL were searched from inception to February 22, 2022. Randomized or non-randomized clinical trials and longitudinal observational studies were eligible for inclusion. Reference screening, data extraction, and risk-of-bias assessment were conducted independently and in duplicate. Publication bias was examined by visual inspection of funnel plots. Meta-analyses were conducted when appropriate using Review Manager 5. The certainty of evidence was assessed using GRADE.

Results

The search identified 1119 references. Of these, 76 papers were selected for full-text assessment and 36 studies (N = 10,882) reported in 39 articles were eligible for inclusion. Older age, higher performance status, and central nervous system involvement were associated with poorer overall survival (OS) and progression-free survival (PFS). Black patients exhibited significantly lower OS and relative survival. Bone marrow involvement and higher albumin levels were associated with poorer OS. Treatment with rituximab, and with methotrexate were associated with better OS and PFS.

Conclusion

This study provides a comprehensive and methodologically rigorous evidence review on PFs in adults with BL. Several significant associations of PFs and survival estimates were observed, therefore, providing data to inform treatment decisions and to improve patient care.

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成人伯基特淋巴瘤患者生存的预后因素:一项系统综述。
伯基特淋巴瘤(BL)是一种罕见的侵袭性非霍奇金淋巴瘤亚型。一些研究已经确定了成年BL患者疾病进展和死亡率的预后因素(PFs)。然而,基于PFs的风险分层尚未达成共识。本研究旨在识别、批判性评估和综合关于PFs对成年bl患者生存的现有证据。方法:进行系统综述。Medline, EMBASE和CENTRAL检索了从创建到2022年2月22日。随机或非随机临床试验和纵向观察性研究符合纳入条件。文献筛选、数据提取和偏倚风险评估是独立进行的,一式两份。发表偏倚采用漏斗图目测检验。在适当的时候使用Review Manager 5进行meta分析。使用GRADE评估证据的确定性。结果:检索到文献1119篇。其中,76篇论文入选全文评估,39篇文章中的36项研究(N = 10,882)入选。年龄越大、表现越好和中枢神经系统受累与总生存期(OS)和无进展生存期(PFS)较差相关。黑人患者表现出明显较低的OS和相对生存率。骨髓受累和较高的白蛋白水平与较差的OS相关。利妥昔单抗和甲氨蝶呤治疗与更好的OS和PFS相关。结论:本研究对成年BL患者的PFs进行了全面且方法严谨的证据回顾。观察到PFs与生存估计的几个重要关联,因此,为指导治疗决策和改善患者护理提供了数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer Medicine
Cancer Medicine ONCOLOGY-
CiteScore
5.50
自引率
2.50%
发文量
907
审稿时长
19 weeks
期刊介绍: Cancer Medicine is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research from global biomedical researchers across the cancer sciences. The journal will consider submissions from all oncologic specialties, including, but not limited to, the following areas: Clinical Cancer Research Translational research ∙ clinical trials ∙ chemotherapy ∙ radiation therapy ∙ surgical therapy ∙ clinical observations ∙ clinical guidelines ∙ genetic consultation ∙ ethical considerations Cancer Biology: Molecular biology ∙ cellular biology ∙ molecular genetics ∙ genomics ∙ immunology ∙ epigenetics ∙ metabolic studies ∙ proteomics ∙ cytopathology ∙ carcinogenesis ∙ drug discovery and delivery. Cancer Prevention: Behavioral science ∙ psychosocial studies ∙ screening ∙ nutrition ∙ epidemiology and prevention ∙ community outreach. Bioinformatics: Gene expressions profiles ∙ gene regulation networks ∙ genome bioinformatics ∙ pathwayanalysis ∙ prognostic biomarkers. Cancer Medicine publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper.
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